日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

AAV-mediated gene transfer of a checkpoint inhibitor in combination with HER2-targeted CAR-NK cells as experimental therapy for glioblastoma

AAV 介导的检查点抑制剂基因转移与 HER2 靶向 CAR-NK 细胞联合用于胶质母细胞瘤的实验性治疗

M I Strecker, K Wlotzka, F Strassheimer, B Roller, G Ludmirski, S König, J Röder, C Opitz, T Alekseeva, J Reul, L Sevenich, T Tonn, W S Wels, J P Steinbach, C J Buchholz, M C Burger

Serotype 1 and 8 Pneumococci Evade Sensing by Inflammasomes in Human Lung Tissue

1型和8型肺炎球菌可逃避人肺组织中炎症小体的识别

Fatykhova, Diana; Rabes, Anne; Machnik, Christoph; Guruprasad, Kunchur; Pache, Florence; Berg, Johanna; Toennies, Mario; Bauer, Torsten T; Schneider, Paul; Schimek, Maria; Eggeling, Stephan; Mitchell, Timothy J; Mitchell, Andrea M; Hilker, Rolf; Hain, Torsten; Suttorp, Norbert; Hippenstiel, Stefan; Hocke, Andreas C; Opitz, Bastian

Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency

利用VAAST基因检测鉴定出一种X连锁遗传疾病,该疾病由于N端乙酰转移酶缺乏而导致男性婴儿死亡。

Rope, Alan F; Wang, Kai; Evjenth, Rune; Xing, Jinchuan; Johnston, Jennifer J; Swensen, Jeffrey J; Johnson, W Evan; Moore, Barry; Huff, Chad D; Bird, Lynne M; Carey, John C; Opitz, John M; Stevens, Cathy A; Jiang, Tao; Schank, Christa; Fain, Heidi Deborah; Robison, Reid; Dalley, Brian; Chin, Steven; South, Sarah T; Pysher, Theodore J; Jorde, Lynn B; Hakonarson, Hakon; Lillehaug, Johan R; Biesecker, Leslie G; Yandell, Mark; Arnesen, Thomas; Lyon, Gholson J

A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signs

一种少汗型外胚层发育不良综合征,伴有牙齿正常、特殊面容、色素紊乱、精神运动和生长发育迟缓、双侧核性白内障及其他体征。

Freire-Maia, N; Fortes, V A; Pereira, L C; Opitz, J M; Marcalle, F A; Cavalli, I J